Overview of common inherited metabolic diseases in a Southern Chinese population of Hong Kong-Reference-Cited by-同舟云学术

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Overview of common inherited metabolic diseases in a Southern Chinese population of Hong Kong

Published:2001-11 Issue:1-2 Volume:313 Page:195-201
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Tang Nelson L.S.,Hui Joannie,Law L.K.,To K.F.,Mak T.W.L.,Cheung K.L.,Vreken Peter,Wanders Ronald J.A.,Fok T.F.

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference37 articles.

1. Incidence of inborn errors of metabolism in British Columbia, 1969–1996;Applegarth;Pediatrics,2000

2. Galactosaemia in Chinese;Kahler;J. Paediatr. Child Health,1999

3. Follow-up study of a nation-wide neonatal metabolic screening program in Japan. A collaborative study group of neonatal screening for inborn errors of metabolism in Japan;Tada;Eur. J. Pediatr.,1984

4. Metabolic disease of the neonate and young infant;Seashore;Semin. Perinatol.,1993

5. Y-chromosome evidence for a northward migration of modern humans into Eastern Asia during the last Ice Age;Su;Am. J. Hum. Genet.,1999

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1. Recurrent rhabdomyolysis and glutaric aciduria type I: a case report and literature review;World Journal of Pediatrics;2016-06-29

2. Inherited metabolic diseases in the Southern Chinese population: spectrum of diseases and estimated incidence from recurrent mutations;Pathology;2014-08

3. Inborn errors of metabolism and expanded newborn screening: review and update;Critical Reviews in Clinical Laboratory Sciences;2013-11

4. Analysis of inborn errors of metabolism: disease spectrum for expanded newborn screening in Hong Kong;CHINESE MED J-PEKING;2011

5. Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency;Clinica Chimica Acta;2009-06

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